## Abstract Acylation of 5โaminoโ3__H__โ1,3,4โthiadiazolinโ2โone (2) was undertaken selectively at either the 3โNH position or at 5โamino group depending on reaction conditions. The 3โNH is highly acidic and acylation takes place with acid anhydrides at this position in high yields in the presence
โฆ LIBER โฆ
Synthesis of 4-acyl-2-(acylamino)-.DELTA.2-1,3,4-thiadiazolines and 4-acyl-2-amino-.DELTA.2-1,3,4-thiadiazolines by acylation of thiosemicarbazones
โ Scribed by Kubota, Seiju; Ueda, Yasufumi; Fujikane, Kazuichi; Toyooka, Kouhei; Shibuya, Masayuki
- Book ID
- 120445673
- Publisher
- American Chemical Society
- Year
- 1980
- Tongue
- English
- Weight
- 681 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-3263
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